- New Recurrent Chromosome Alterations in Patients with Multiple Myeloma and Plasma Cell Leukemia
[作者:Stella, F; Pedrazzini, E; Rodriguez, A; Baialardo, E; Kusminsky, G; Arbelbide, J; Fantl, DB; Slavutsky, I,期刊:Cytogenetic and Genome Research, 页码:249-259 , 文章类型: Article,,卷期:2011年134-4]
- Chromosome abnormalities detected in metaphases from multiple myeloma (MM) cells have a clear impact on prognosis and response to therapy. Thirteen out of 50 (26%) patients with plasma cell disorders and abnormal karyoty...
- Identification of Copy Number Variants on Human Chromosome 22 in Patients with a Variety of Clinical Findings
[作者:Yu, S; Graf, WD; Ramalingam, A; Brawner, SJ; Joyce, JM; Fiedler, S; Zhou, XG; Liu, HY,期刊:Cytogenetic and Genome Research, 页码:260-268 , 文章类型: Article,,卷期:2011年134-4]
- The aims of this study were to create a copy number variant (CNV) profile of human chromosome 22 and to establish a genotype-phenotype correlation for patients with genomic abnormalities on chromosome 22. Thus, 1,654 con...
- Overexpression of Lis1 in Different Stages of Spermatogenesis Does Not Result in an Aberrant Phenotype
[作者:Drusenheimer, N; Nayernia, K; Meinhardt, A; Jung, B; Arnold, HH; Engel, W,期刊:Cytogenetic and Genome Research, 页码:269-282 , 文章类型: Article,,卷期:2011年134-4]
- Previous studies showed that in the mouse mutant Lis1(GT/GT) gene trap integration in intron 2 of Lis1 gene leads to male infertility in homozygous Lis1(GT/GT) mice. We further analyzed this line and could confirm the su...
- Cytotaxonomy, Morphology and Ecology of the Simulium nobile Species Group (Diptera: Simuliidae) in Thailand
[作者:Tangkawanit, U; Kuvangkadilok, C; Trinachartvanit, W; Baimai, V,期刊:Cytogenetic and Genome Research, 页码:308-318 , 文章类型: Article,,卷期:2011年134-4]
- The polytene chromosomes of 512 larvae of the Simulium nobile species group collected from 16 stream sites in northern, central and southern Thailand were examined. Band-by-band comparisons relative to the established st...
- Genome-Wide Analysis of Sox Genes in Medaka (Oryzias latipes) and Their Expression Pattern in Embryonic Development
[作者:Cui, J; Shen, X; Zhao, H; Nagahama, Y,期刊:Cytogenetic and Genome Research, 页码:283-294 , 文章类型: Article,,卷期:2011年134-4]
- Genes of the Sox family encode evolutionarily conserved high-mobility group box containing transcription factors, which play key roles in various events of developmental contexts. In this study, we identified 15 sox gene...
- Chromosomal Distribution of Repetitive DNA Sequences Highlights the Independent Differentiation of Multiple Sex Chromosomes in Two Closely Related Fish Species
[作者:Cioffi, MB; Molina, WF; Moreira, O; Bertollo, LAC,期刊:Cytogenetic and Genome Research, 页码:295-302 , 文章类型: Article,,卷期:2011年134-4]
- The arrangement of 6 repetitive DNA sequences in the mitotic and meiotic sex chromosomes of 2 Erythrinidae fish, namely Hoplias malabaricus and Erythrinus erythrinus, both with a multiple X1X1X2X2/X1X2Y sex chromosome sy...
- Physical Mapping of 5S rDNA in Two Species of Knifefishes: Gymnotus pantanal and Gymnotus paraguensis (Gymnotiformes)
[作者:da Silva, M; Matoso, DA; Vicari, MR; de Almeida, MC; Margarido, VP; Artoni, RF,期刊:Cytogenetic and Genome Research, 页码:303-307 , 文章类型: Article,,卷期:2011年134-4]
- Physical mapping of 5S rDNA in 2 species of knifefishes, Gymnotus pantanal and G. paraguensis (Gymnotiformes), was performed using fluorescence in situ hybridization with a 5S rDNA probe. The 5S rDNA PCR product from the...
- Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmental Delay: A Case Report
[作者:Tan, EC; Lim, E; Cham, B; Knight, L; Ng, I,期刊:Cytogenetic and Genome Research, 页码:319-324 , 文章类型: Article,,卷期:2011年134-4]
- Unbalanced translocation involving both chromosome 3p duplication and 11q deletion in the same patient is extremely rare; only 1 live-born case was reported previously. This karyotype was also detected during prenatal di...
- Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature
[作者:Guilherme, RS; Bragagnolo, S; Pellegrino, R; Christofolini, DM; Takeno, SS; Carvolheira, GM; Kulikowski, LD; Melaragno, MI,期刊:Cytogenetic and Genome Research, 页码:325-330 , 文章类型: Review,,卷期:2011年134-4]
- Ring chromosome 3 is a rare abnormality with only 10 patients described in the literature. We report a patient with r(3) and similar to 6-Mb distal 3p deletion. Single nucleotide polymorphism array, multiplex ligation-de...
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